HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992685Generated: October 26, 2026
Triphenylphosphine → 4-(Benzoylthiomethyl)-1-methylpyrazole
https://huagongshe.com/reaction/992685
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | (1-methyl-1H-pyrazol-4-yl)methanol | HCID 11961423 | — |
| Reactant | HCID 178526132 | HCID 178526132 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(Benzoylthiomethyl)-1-methylpyrazole | HCID 18411601 | — |
Reaction Steps
Under nitrogen atmosphere, 78.7 g of triphenylphosphine (300 m mol) and 47.2 ml of diethyl azodicarboxylate (300 m mol) were added to a stirred solution of 22.4 g of 4-hydroxymethyl-1-methylpyrazole (200 m mol) in THF (250 ml) at 5° C. After stirring for 1 hour at the same temperature, 42.3 ml of thiobenzoic acid (360 m mol) was added slowly to the mixture. The mixture was poured into a mixture of water and ethyl acetate, while Ph was adjusted to 9.5 with 30% potassium bicarbonate. Aqueous layer was separated, the organic layer was washed with brine, dried over magnesium sulfate. After filtration of the mixture, the filtrate was concentrated in vacuo, and the residue was purified on silica gel (eluent: n-hexane-ethyl acetate) to afford 4-(benzoylthiomethyl)-1-methylpyrazole (18.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06468995B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-1973982b4d134b29b792487866876acc |
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| Source note | uspto-grants-2002_10 |
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